De Cruppe 2005.
Methods | Randomised controlled trial of consultation liaison compared to standard care. | |
Participants | Consumers (n = 67): consumers referred to a hospital‐based psychosomatic consultation liaison service. Their mean age was 45 years, 42% were male. Somatoform disorders 21, common psychiatric disorders 22, and adjustment disorder or stress reaction 24. Excluded: organic mental disorders; substance‐ and abuse‐related disorders, schizophrenia, schizotypal or delusional disorders, pre‐terminal illness or limited German. Primary care providers (n not reported): general practitioners of a consumer randomised to the intervention group, 62.4% had received certification for psychosomatic primary care. Mental health specialists (n = 5): psychosomatic consultants trained in internal medicine and psychotherapy with one year training. Setting: GP practices in Germany 1998‐9. |
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Interventions | 1. Consultation Liaison (n = 33) Mental health specialist/consumer: initial assessment through hospital psychosomatic consultation liaison service and recommendation for further psychosocial care and therapy. Mental health specialist/primary care provider: one phone‐call (10 min) and one written report. Both incorporated diagnosis, symptom‐related psychosocial findings and therapy recommendations. Primary care provider/consumer: recommendations were made to primary care providers to hold symptom‐based conversations with the client integrating psychosocial aspects every four to six weeks. 2. Standard care (n = 34) Mental health specialist/consumer: initial assessment through hospital psychosomatic consultation liaison service and recommendation for further psychosocial care and therapy (as for consultation liaison). |
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Outcomes | 1. Consumer Symptoms: Beschwerden Liste (general and somatic symptoms, 24 item), Allgemeine Depressionskala (Depressive symptoms, 20 item), State‐Trait Anxiety Inventory (20 item), WHO Global Assessment of Social Functioning (five‐point scale) at 6 and 42 months. Adherence: used recommended psychotherapy treatments at 6 and 42 months. 2. Provider Adherence: followed through with CL recommendations over 6 months. |
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Notes | As provider sample sizes were not reported, these were assumed to be the same as consumers for provider adherence. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | An independent statistician block randomised consumers by diagnosis. |
Allocation concealment (selection bias) | Low risk | See sequence generation. |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Independent statistician was responsible for psychometric tests but responses were self‐reported; however, participants probably did not know whether they were in the active group. |
Incomplete outcome data (attrition bias) All outcomes | High risk | Data was reported for those available at follow‐up, loss to follow‐up at 6 months 21%, 42 months 28%. |
Selective reporting (reporting bias) | High risk | The only consumer outcome reported was use of psychotherapies. Primary care provider adherence was reported but sample sizes were not reported. |
Other bias | Unclear risk | No other bias identified. |